Hippocampal metabolic profile during epileptogenesis in the pilocarpine model of epilepsy

Author:

Meier Letícia12ORCID,Bruginski Estevan12,Marafiga Joseane Righes34,Caus Letícia Barbieri3,Pasquetti Mayara Vendramin3,Calcagnotto Maria Elisa34,Campos Francinete Ramos12

Affiliation:

1. Biosciences and Mass Spectrometry Laboratory, Department of Pharmacy Universidade Federal do Paraná Curitiba PR Brazil

2. Graduate Program in Pharmaceutical Science Universidade Federal do Paraná Curitiba PR Brazil

3. Neurophysiology and Neurochemistry of Neuronal Excitability and Synaptic Plasticity Laboratory (NNNESP Lab.), Department of Biochemistry, ICBS Universidade Federal do Rio Grande do Sul Porto Alegre RS Brazil

4. Graduate Program in Biological Science: Biochemistry Universidade Federal do Rio Grande do Sul Porto Alegre RS Brazil

Abstract

AbstractTemporal lobe epilepsy (TLE) is a common form of refractory epilepsy in adulthood. The metabolic profile of epileptogenesis is still poorly investigated. Elucidation of such a metabolic profile using animal models of epilepsy could help identify new metabolites and pathways involved in the mechanisms of epileptogenesis process. In this study, we evaluated the metabolic profile during the epileptogenesis periods. Using a pilocarpine model of epilepsy, we analyzed the global metabolic profile of hippocampal extracts by untargeted metabolomics based on ultra‐performance liquid chromatography–high‐resolution mass spectrometry, at three time points (3 h, 1 week, and 2 weeks) after status epilepticus (SE) induction. We demonstrated that epileptogenesis periods presented different hippocampal metabolic profiles, including alterations of metabolic pathways of amino acids and lipid metabolism. Six putative metabolites (tryptophan, N‐acetylornithine, N‐acetyl‐L‐aspartate, glutamine, adenosine, and cholesterol) showed significant different levels during epileptogenesis compared to their respective controls. These putative metabolites could be associated with the imbalance of neurotransmitters, mitochondrial dysfunction, and cell loss observed during both epileptogenesis and epilepsy. With these findings, we provided an overview of hippocampal metabolic profiles during different stages of epileptogenesis that could help investigate pathways and respective metabolites as predictive tools in epilepsy.

Publisher

Wiley

Subject

Clinical Biochemistry,Drug Discovery,Pharmacology,Molecular Biology,General Medicine,Biochemistry,Analytical Chemistry

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